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Noninvasive stool-based detection of infant gastrointestinal development using gene expression profiles from exfoliated epithelial cells

机译:基于脱落的上皮细胞的基因表达谱基于粪便的非侵入性粪便检测

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摘要

We have developed a novel molecular methodology that utilizes stool samples containing intact sloughed epithelial cells to quantify intestinal gene expression profiles in the developing human neonate. Since nutrition exerts a major role in regulating neonatal intestinal development and function, our goal was to identify gene sets (combinations) that are differentially regulated in response to infant feeding. For this purpose, fecal mRNA was isolated from exclusively breast-fed (n = 12) and formula-fed (n = 10) infants at 3 mo of age. Linear discriminant analysis was successfully used to identify the single genes and the two- to three-gene combinations that best distinguish the feeding groups. In addition, putative “master” regulatory genes were identified using coefficient of determination analysis. These results support our premise that mRNA isolated from stool has value in terms of characterizing the epigenetic mechanisms underlying the developmentally regulated transcriptional activation/repression of genes known to modulate gastrointestinal function. As larger data sets become available, this methodology can be extended to validation and, ultimately, identification of the main nutritional components that modulate intestinal maturation and function.
机译:我们已经开发出一种新颖的分子方法,该方法利用含有完整脱落的上皮细胞的粪便样本来量化发育中的人类新生儿的肠道基因表达谱。由于营养在调节新生儿肠道发育和功能中起着重要作用,因此我们的目标是确定响应婴儿喂养而受到差异调节的基因集(组合)。为此,从3个月大的母乳喂养(n = 12)和配方喂养(n = 10)的婴儿中分离出粪便mRNA。线性判别分析已成功用于鉴定最能区分饲养组的单个基因和两个至三个基因的组合。另外,使用确定系数分析鉴定了假定的“主”调控基因。这些结果支持了我们的前提,即从粪便中分离出的mRNA具有表征表观遗传机制的价值,该表观遗传机制是已知调节胃肠功能的基因的发育调控的转录激活/抑制的基础。随着更大数据集的获得,这种方法可以扩展到验证,最终确定调节肠道成熟和功能的主要营养成分。

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